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评估肥胖患者基于体重的依诺肝素给药对抗-Xa 浓度的影响。

Evaluation of weight based enoxaparin dosing on anti-Xa concentrations in patients with obesity.

机构信息

Princess Alexandra Hospital, Brisbane, Australia.

The University of Queensland, Brisbane, Australia.

出版信息

J Thromb Thrombolysis. 2019 Oct;48(3):387-393. doi: 10.1007/s11239-019-01847-4.

Abstract

Current treatment dose of enoxaparin is based on total body weight (TBW), however dosage in obesity remains unclear. "Dose capping" commonly occurs if TBW > 100 kg minimising bleeding risk. However, this may result in under-dosing and increasing embolisation risk. The primary objective evaluated efficacy of current dosing strategies in obese patients and determined if resultant anti-Xa concentrations (aXaC) were therapeutic. The secondary objective was to investigate if an uncapped 0.75-0.85 mg/kg (TBW) twice daily dose, advocated by previous authors, results in therapeutic aXaC (0.5-1.0 IU/ml). This retrospective study included 133 patients with a median TBW of 128 kg, producing 59% therapeutic, 15% sub-therapeutic and 26% supra-therapeutic aXaC. Approximately 60% of patients in each dose group (< 0.75, 0.75-0.85 and > 0.85 mg/kg) had a therapeutic aXaC, however the percentage of sub-therapeutic versus supra-therapeutic was higher in the < 0.75 (27% vs 9%) and > 0.85 mg/kg (10% vs 34%) groups respectively. Most patients who weighed 100-119 kg (TBW) received doses > 0.85 mg/kg, however 32% had toxic aXaC. Those between 120 and 139 kg (TBW) had a high percentage of therapeutic aXaC (87%) when dosed < 0.75 mg/kg and a high percentage of supra-therapeutic aXaC (71%) when dosed > 0.85 mg/kg; although numbers were low. Dose reduction occurred in patients > 140 kg (TBW), however < 0.75 mg/kg resulted in higher percentage of sub-therapeutic aXaC (42%). Dosing at 0.75-0.85 mg/kg results in 62% of therapeutic, 14% sub-therapeutic and 24% supra-therapeutic aXaC. This appears to be a "safe" starting dose-range, however all obese patients should have aXaC monitoring due to high inter-patient variability.

摘要

目前依诺肝素的治疗剂量是基于总体重(TBW),但肥胖患者的剂量仍不明确。如果 TBW>100kg,则通常会“剂量封顶”,以最小化出血风险。然而,这可能导致剂量不足和增加栓塞风险。本研究的主要目的是评估肥胖患者中当前剂量方案的疗效,并确定所得抗 Xa 浓度(aXaC)是否具有治疗作用。次要目的是研究以前作者提倡的 0.75-0.85mg/kg(TBW)、每日两次的未封顶剂量是否会产生治疗性 aXaC(0.5-1.0IU/ml)。这项回顾性研究纳入了 133 名 TBW 中位数为 128kg 的患者,产生了 59%的治疗性、15%的亚治疗性和 26%的超治疗性 aXaC。<0.75、0.75-0.85 和>0.85mg/kg 三个剂量组中约有 60%的患者具有治疗性 aXaC,然而,<0.75(27%比 9%)和>0.85mg/kg(10%比 34%)组中超治疗性与亚治疗性的比例更高。大多数体重为 100-119kg(TBW)的患者接受了>0.85mg/kg 的剂量,但 32%的患者存在毒性 aXaC。体重为 120-139kg(TBW)的患者接受<0.75mg/kg 剂量时,治疗性 aXaC 的比例较高(87%),接受>0.85mg/kg 剂量时,超治疗性 aXaC 的比例较高(71%);尽管数量较少。体重>140kg(TBW)的患者会减少剂量,但<0.75mg/kg 会导致更高比例的亚治疗性 aXaC(42%)。0.75-0.85mg/kg 的剂量会产生 62%的治疗性、14%的亚治疗性和 24%的超治疗性 aXaC。这似乎是一个“安全”的起始剂量范围,但由于患者间存在高度变异性,所有肥胖患者都应进行 aXaC 监测。

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